School of Life Sciences, South China Normal University, Guangzhou 510631, China.
College of Biophotonics, South China Normal University, Guangzhou 510631, China.
Nano Lett. 2021 Jun 9;21(11):4643-4653. doi: 10.1021/acs.nanolett.1c00715. Epub 2021 May 26.
DNA quantification is important for biomedical research, but the routinely used techniques rely on nucleic acid amplification which have inherent issues like cross-contamination risk and quantification bias. Here, we report a CRISPR-Cas12a-based molecular diagnostic technique for amplification-free and absolute quantification of DNA at the single-molecule level. To achieve this, we first screened out the optimal reaction parameters for high-efficient Cas12a assay, yielding over 50-fold improvement in sensitivity compared with the reported Cas12a assays. We further leveraged the microdroplet-enabled confinement effect to perform an ultralocalized droplet Cas12a assay, obtaining excellent specificity and single-molecule sensitivity. Moreover, we demonstrated its versatility and quantification capability by direct counting of diverse virus's DNAs (African swine fever virus, Epstein-Barr virus, and Hepatitis B virus) from clinical serum samples with a wide range of viral titers. Given the flexible programmability of crRNA, we envision this amplification-free technique as a versatile and quantitative platform for molecular diagnosis.
DNA 定量对于生物医学研究非常重要,但常用的技术依赖于核酸扩增,而核酸扩增存在交叉污染风险和定量偏差等固有问题。在这里,我们报告了一种基于 CRISPR-Cas12a 的分子诊断技术,用于在单分子水平上进行无扩增和绝对定量的 DNA。为了实现这一目标,我们首先筛选出高效 Cas12a 测定的最佳反应参数,与已报道的 Cas12a 测定相比,灵敏度提高了 50 多倍。我们进一步利用微滴技术实现了超局部化的液滴 Cas12a 测定,获得了优异的特异性和单分子灵敏度。此外,我们通过直接计数来自临床血清样本中不同病毒(非洲猪瘟病毒、爱泼斯坦-巴尔病毒和乙型肝炎病毒)的 DNA,证明了其多功能性和定量能力,病毒滴度范围很广。鉴于 crRNA 的灵活可编程性,我们设想这种无扩增技术是一种用于分子诊断的通用和定量平台。